Clopidogrel Plus Aspirin Versus Warfarin in Patients With Stroke and Aortic Arch Plaques

被引:124
|
作者
Amarenco, Pierre [1 ]
Davis, Stephen [5 ]
Jones, Elizabeth F. [7 ]
Cohen, Ariel A. [2 ,3 ]
Heiss, Wolf-Dieter [8 ]
Kaste, Markku [9 ]
Laouenan, Cedric [4 ]
Young, Dennis [6 ,10 ]
Macleod, Malcolm [6 ,11 ]
Donnan, Geoffrey A. [6 ]
机构
[1] Paris Diderot Sorbonne Univ, Hop Bichat, INSERM, Dept Neurol,Stroke Ctr,DHU FIRE,U1148, Paris, France
[2] Univ Paris 06, Dept Cardiol, St Antoine Hosp, Paris, France
[3] Univ Paris 06, Sch Med, Paris, France
[4] Paris Diderot Sorbonne Univ, Hop Bichat, Assistance Publ Hop Paris, Dept Biostat, Paris, France
[5] Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic, Australia
[6] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia
[7] Austin Hlth, Dept Cardiol, Heidelberg, Vic, Australia
[8] Max Planck Inst Neurol Res, D-50931 Cologne, Germany
[9] Univ Helsinki, Cent Hosp, Dept Neurol, Helsinki, Finland
[10] Monash Univ, Stroke & Ageing Res Ctr, Melbourne, Vic 3004, Australia
[11] Univ Edinburgh SC005336, Div Clin Neurosci, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
aorta; atherosclerosis; cerebral infarction; TRANSIENT ISCHEMIC ATTACK; VASCULAR EVENTS; DOUBLE-BLIND; RISK-FACTOR; FOLLOW-UP; ATHEROMAS; ATHEROSCLEROSIS; PREVENTION; MATCH;
D O I
10.1161/STROKEAHA.113.004251
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose Severe atherosclerosis in the aortic arch is associated with a high risk of recurrent vascular events, but the optimal antithrombotic strategy is unclear. Methods This prospective randomized controlled, open-labeled trial, with blinded end point evaluation (PROBE design) tested superiority of aspirin 75 to 150 mg/d plus clopidogrel 75 mg/d (A+C) over warfarin therapy (international normalized ratio 2-3) in patients with ischemic stroke, transient ischemic attack, or peripheral embolism with plaque in the thoracic aorta >4 mm and no other identified embolic source. The primary end point included cerebral infarction, myocardial infarction, peripheral embolism, vascular death, or intracranial hemorrhage. Follow-up visits occurred at 1 month and then every 4 months post randomization. Results The trial was stopped after 349 patients were randomized during a period of 8 years and 3 months. After a median follow-up of 3.4 years, the primary end point occurred in 7.6% (13/172) and 11.3% (20/177) of patients on A+C and on warfarin, respectively (log-rank, P=0.2). The adjusted hazard ratio was 0.76 (95% confidence interval, 0.36-1.61; P=0.5). Major hemorrhages including intracranial hemorrhages occurred in 4 and 6 patients in the A+C and warfarin groups, respectively. Vascular deaths occurred in 0 patients in A+C arm compared with 6 (3.4%) patients in the warfarin arm (log-rank, P=0.013). Time in therapeutic range (67% of the time for international normalized ratio 2-3) analysis by tertiles showed no significant differences across groups. Conclusions Because of lack of power, this trial was inconclusive and results should be taken as hypothesis generating. Clinical Trial Registration URL: http://www.clinicaltrials.gov. Unique identifier: NCT00235248.
引用
收藏
页码:1248 / 1257
页数:10
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